Canonical Allele Identifier: CA2260099661

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612254C= , CM000679.2:g.41612254C=	GRCh38
NC_000017.10:g.39768506C= , CM000679.1:g.39768506C=	GRCh37
NC_000017.9:g.37022032C=	NCBI36
NG_008301.1:g.5574G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.435G= MANE Select	ENSP00000301653.3:p.Leu145=
ENST00000301653.8:c.435G=	ENSP00000301653.3:p.Leu145=
ENST00000588319.1:n.512G=
ENST00000593067.1:c.-280G=	ENSP00000467124.1:n.-280G=
NM_005557.3:c.435G=	NP_005548.2:p.Leu145=
NM_005557.4:c.435G= MANE Select	NP_005548.2:p.Leu145=